RecruitingNCT04707794

Incidence of Postoperative Delirium in Elderly Patients Undergoing Non-cardiac Surgery

The Incidence, Risk Factors and Outcome of Postoperative Delirium in Elderly Patients Undergoing Non-cardiac Surgery: a Prospective Observational Study


Sponsor

Sir Ganga Ram Hospital

Enrollment

270 participants

Start Date

Jan 14, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

Postoperative delirium (POD) is the most common adverse neurologic complication that can occur in patients of any age. Its incidence varies across age groups and is substantially influenced by patient-related risk factors. POD occurs in 17%-61% of major surgical procedures. Several risk factors which contribute to the development of POD include age more than 60 years, pre-existing cognitive dysfunction, presence of comorbidities, sensorial deficits, malnutrition, polypharmacy, impaired physical mobility and frailty. Postoperative delirium has several wide ranging and adverse outcomes that are consistently associated with delirium such as mortality, increased length of hospital stay, and increased hospital costs. A recently devised tool for rapid assessment of delirium is the 4 A's test. It has now been validated for identifying delirium in the surgical population. The proposed prospective observational study will be conducted on 150 patients belonging to ASA Physical Status I-III of either sex, scheduled to undergo non-cardiac surgery under general anaesthesia (GA), requiring at least 24 hours of postoperative inpatient care. This prospective, observational study aims to evaluate the incidence, risk factors and outcomes of postoperative delirium in elderly patients more than 65 years of age undergoing non-cardiac surgery.


Eligibility

Min Age: 65 Years

Inclusion Criteria6

  • Patients of age >65yrs
  • Either sex
  • ASA physical status I - III
  • Elective non-cardiac surgical procedures under general anesthesia
  • Clinical Frailty Score (CFS): 1-8
  • Patients requiring at least 24 hours of postoperative inpatient care.

Exclusion Criteria9

  • Clinical Frailty Score (CFS) of 9
  • Patients diagnosed with dementia, severe psychiatric or neurological diseases
  • Recent surgery within past 3-months
  • History of recent head injury in the preceding 3 months
  • Patients with uncompensated cardiovascular disease, hepato-renal insufficiency and uncontrolled endocrine disease
  • Patients on anti-depressant, anti-anxiety, anti-convulsant and anti-parkinsonism medications
  • Preoperative haemoglobin < 8 gm % and serum albumin < 3.5mg/dl
  • Patient inability to give informed consent
  • Presence of preoperative delirium as assessed by 4A'S Test (score ≥ 4)

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGSevoflurane

Sevoflurane delivery will will be titrated to maintain anaesthesia depth of 50 (BIS score) using bispectral (BIS) index monitioring

DRUGDesflurane

Desflurane delivery will be titrated to maintain anaesthesia depth of 50 (BIS score) using bispectral (BIS) index monitioring


Locations(2)

Sir Ganga Ram Hospital

New Delhi, National Capital Territory of Delhi, India

Sir Ganga Ram Hospital

New Delhi, India

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04707794


Related Trials